Canonical Allele Identifier: CA1981486982

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435721A= , CM000673.2:g.71435721A=	GRCh38
NC_000011.9:g.71146767A= , CM000673.1:g.71146767A=	GRCh37
NC_000011.8:g.70824415A=	NCBI36
NG_012655.2:g.17711T= , LRG_340:g.17711T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1082T=	ENSP00000435707.3:p.Phe361=
ENST00000526780.6:c.1082T=	ENSP00000435668.2:p.Phe361=
ENST00000527316.6:c.908T=	ENSP00000435047.2:p.Phe303=
ENST00000682708.1:c.1133T=	ENSP00000506866.1:p.Phe378=
ENST00000683287.1:c.1118T=	ENSP00000507607.1:p.Phe373=
ENST00000683714.1:c.1090T=	ENSP00000508207.1:p.Ser364=
ENST00000684396.1:n.1122T=
ENST00000685320.1:c.497T=	ENSP00000509319.1:p.Phe166=
ENST00000690257.1:c.986T=	ENSP00000510750.1:p.Phe329=
ENST00000355527.8:c.1082T= MANE Select	ENSP00000347717.4:p.Phe361=
ENST00000355527.7:c.1082T=	ENSP00000347717.3:p.Phe361=
ENST00000407721.6:c.1082T=	ENSP00000384739.2:p.Phe361=
ENST00000525137.1:c.583T=	ENSP00000435956.1:p.Ser195=
ENST00000533800.5:c.332T=	ENSP00000435011.1:p.Phe111=
ENST00000534795.5:c.319+2091T=
NM_001163817.1:c.1082T=	NP_001157289.1:p.Phe361=
NM_001360.2:c.1082T= , LRG_340t1:c.1082T=	NP_001351.2:p.Phe361=
XM_011544777.1:c.1216T=	XP_011543079.1:p.Ser406=
XM_011544777.2:c.1216T=	XP_011543079.1:p.Ser406=
NM_001163817.2:c.1082T=	NP_001157289.1:p.Phe361=
NM_001360.3:c.1082T= MANE Select	NP_001351.2:p.Phe361=